DeepRaccess:使用深度学习进行高速RNA可及性预测。

IF 2.8 Q2 MATHEMATICAL & COMPUTATIONAL BIOLOGY Frontiers in bioinformatics Pub Date : 2023-10-10 eCollection Date: 2023-01-01 DOI:10.3389/fbinf.2023.1275787
Kaisei Hara, Natsuki Iwano, Tsukasa Fukunaga, Michiaki Hamada
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引用次数: 0

摘要

RNA可及性是预测原核生物中RNA-RNA相互作用和翻译效率的有用的RNA二级结构特征。然而,传统的可访问性计算工具,如Raccess,在计算上是昂贵的,并且需要相当长的计算时间来执行转录组规模的分析。在这项研究中,我们开发了DeepRaccess,它基于深度学习方法预测RNA的可及性。训练DeepRaccess以人工RNA序列作为输入,并预测Raccess计算的这些序列的可访问性。仿真和经验数据集分析表明,DeepRaccess预测的可达性与Raccess计算的可达性高度相关。此外,我们证实DeepRaccess可以从起始密码子周围的序列中以中等精度预测大肠杆菌中的蛋白质丰度。我们还证明了DeepRaccess在GPU环境中实现了数十到数百倍的软件加速。DeepRaccess的源代码和经过训练的模型可在https://github.com/hmdlab/DeepRaccess.
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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DeepRaccess: high-speed RNA accessibility prediction using deep learning.

RNA accessibility is a useful RNA secondary structural feature for predicting RNA-RNA interactions and translation efficiency in prokaryotes. However, conventional accessibility calculation tools, such as Raccess, are computationally expensive and require considerable computational time to perform transcriptome-scale analysis. In this study, we developed DeepRaccess, which predicts RNA accessibility based on deep learning methods. DeepRaccess was trained to take artificial RNA sequences as input and to predict the accessibility of these sequences as calculated by Raccess. Simulation and empirical dataset analyses showed that the accessibility predicted by DeepRaccess was highly correlated with the accessibility calculated by Raccess. In addition, we confirmed that DeepRaccess could predict protein abundance in E.coli with moderate accuracy from the sequences around the start codon. We also demonstrated that DeepRaccess achieved tens to hundreds of times software speed-up in a GPU environment. The source codes and the trained models of DeepRaccess are freely available at https://github.com/hmdlab/DeepRaccess.

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